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Ce Approved Auto Hematology Analyzer (WHY6580)
US$1,500.00-3,000.00
1 Piece

Product profile

Customization

Available

Classification

Biological Diagnostics

Type

Urine Analyzer

Model NO.

WHY6580

Certification

CE, ISO13485

Group

Neonatal, Child and Adult

Standard Working Model

Dual-Channel Testing

Aperture

Wbc 80um Rbc/Plt 50um

Power Supply

AC220V-230V/50Hz or AC110V-1200V/50-60Hz

Input / Output

4USB and Bi-Directional Lis Connection

Results Storage

Storage of 50, 000 Patients' Results

Sample Quantity

9UL Venous Blood, 20UL Pre-Dilution Blood

Principle

Electrical Impedance for Counting and Sft Method F

Display

10.4 " Color LCD

Calibration

Manual and Automatic Calibration

Transport Package

Wooden Pallet

Specification

ISO, CE, FDA, FSC

Trademark

Poweam

Origin

China

HS Code

90278099

Production Capacity

800PCS/Month

Key features

High Throughput Speed: Processes up to 60 samples per hour with automatic sampling.
Dual-Channel Testing: Separate WBC and RBC units ensure accurate results and reduce cross-contamination.
Large Data Storage: Stores up to 50,000 patient results including histograms for easy review.
Advanced Display: Features a 10.4-inch large color LCD touch screen for easy operation.
CE & ISO Certified: Meets CE and ISO13485 standards for safety and quality assurance.
Automatic Dilution: Internal diluter adds 1ml diluent automatically to avoid manual errors.
Comprehensive QC: Includes comprehensive QC program with automatic histogram printing.
Flexible Connectivity: Supports 4 USB ports and bi-directional LIS connection for data management.

Company profile

Business Type: Manufacturer/FactoryExport Year: 2003-03-01Nearest Port: shanghai,ningboAverage Response Time: ≤24hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, CIP, CPT, Others

AI-Powered supplier vetting

SummaryNanjing Poweam Medical Co., Ltd. is identified as a China-based manufacturer/factory in Nanjing, Jiangsu, focused on medical equipment including ultrasound, X-ray, ECG, IVD, microscope, and related products. The supplier reports ISO 9000, ISO 13485, and ISO 9001 certifications, more than 10 production lines, 50 R&D engineers, 50 quality-control staff, and stated technical support, training, installation backup, and registration assistance. It has exported since 2003 and serves multiple global regions, with stated order fulfillment within 15 working days in both peak and off-peak periods. However, the available trade records show only one transaction for each of two closely related microscope listings, so customer-case depth is limited. No sufficient evidence is provided to assess financial credibility, product customization, or measurable innovation output.
Supplier typeThe supplier is explicitly identified as a Manufacturer/Factory and a wholly foreign-owned enterprise located in Nanjing, China. Its stated business covers health and medicine and a broad range of medical equipment, supporting classification as a medical-device manufacturer rather than only a trading company.
CertificationsThe supplier reports holding ISO 9000, ISO 13485, and ISO 9001 management-system certifications. ISO 13485 is specifically relevant to medical-device quality management, providing explicit positive evidence for this field.
After-Sales capabilityThe supplier states that it provides on-the-ground launch assistance, product advice, equipment and installation training, technical-engineer support, backup, registration facilitation, and relevant certificates when necessary. Its export experience since 2003 and stated global market coverage further support service experience, although no service-response metrics are provided.
Production capacityThe supplier reports more than 10 production lines, 50 quality-control staff, and stated fulfillment within 15 working days in both peak and off-peak seasons. These explicit capacity and delivery statements support a positive assessment, although actual capacity by product category is not specified.

Product Q&A

Q:What is the testing throughput?
A:
The analyzer can process up to 60 samples per hour with automatic sampling capabilities.
Q:How many patient results can be stored?
A:
It can store up to 50,000 patient results, including histograms, for convenient management and review.
Q:What certifications does the device have?
A:
The device is certified with CE and ISO13485 standards.
Q:Does it require manual diluent addition?
A:
No, it features an internal diluter that automatically adds 1ml of diluent to avoid manual errors.
Q:What is the sample quantity required?
A:
It requires 9ul of venous blood or 20ul of pre-dilution blood.

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